Significance of localized expression of full-length growth differentiation factor-15 in cachexia of advanced non-small cell lung cancer

Purpose Growth differentiation factor-15 (GDF-15) is one of the key cachexia-inducing factors. Clinical trials on therapies targeting GDF-15 for cancer and cancer cachexia are underway. While the role of circulating GDF-15 in cachexia has been clarified, the effects of GDF-15 expression within cance...

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Veröffentlicht in:Supportive care in cancer 2023-05, Vol.31 (5), p.308-308, Article 308
Hauptverfasser: Morita-Tanaka, Satomi, Miyagawa-Hayashino, Aya, Yamada, Tadaaki, Matsui, Yohei, Morimoto, Kenji, Hiranuma, Osamu, Masuzawa, Naoko, Yoshimura, Akihiro, Iwasaku, Masahiro, Tokuda, Shinsaku, Kaneko, Yoshiko, Kim, Young Hak, Konishi, Eiichi, Takayama, Koichi
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Sprache:eng
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Zusammenfassung:Purpose Growth differentiation factor-15 (GDF-15) is one of the key cachexia-inducing factors. Clinical trials on therapies targeting GDF-15 for cancer and cancer cachexia are underway. While the role of circulating GDF-15 in cachexia has been clarified, the effects of GDF-15 expression within cancer cells remain to be fully elucidated. Hence, the objective of this study was to investigate the expression of GDF-15 in advanced lung cancer tissues and to understand its role in cachexia. Methods We retrospectively examined the expression level of full-length GDF-15 in advanced non-small cell lung cancer tissues and analyzed the relationship between the staining intensity and clinical data in 53 samples. Results We found that 52.8% of the total samples were GDF-15 positive, and GDF-15 expression significantly correlated with improved C-reactive protein/albumin ratio ( p  = 0.008). It did not correlate with the existence of cancer cachexia and overall survival ( p  = 0.43). Conclusion Our findings show that GDF-15 expression significantly correlated with improved C-reactive protein/albumin ratio, but not the existence of cancer cachexia in advanced NSCLC patients.
ISSN:0941-4355
1433-7339
DOI:10.1007/s00520-023-07771-x